Canonical Allele Identifier: PA2826658929
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 3070634
ClinVar RCV Id: RCV004013144
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269554.1:p.Ile299Phe
CA342817805
NM_001282625.2:c.895A>T